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Equate omeprazole delayed release - 49035-915-03 - (Omeprazole)

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Drug Information of Equate omeprazole delayed release

Product NDC: 49035-915
Proprietary Name: Equate omeprazole delayed release
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Equate omeprazole delayed release

Product NDC: 49035-915
Labeler Name: Wal-Mart Stores Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080227

Package Information of Equate omeprazole delayed release

Package NDC: 49035-915-03
Package Description: 3 BOTTLE in 1 CARTON (49035-915-03) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE

NDC Information of Equate omeprazole delayed release

NDC Code 49035-915-03
Proprietary Name Equate omeprazole delayed release
Package Description 3 BOTTLE in 1 CARTON (49035-915-03) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC 49035-915
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080227
Marketing Category Name NDA
Labeler Name Wal-Mart Stores Inc
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Equate omeprazole delayed release


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